AI, Language and Healthcare

It’s only natural that as AI technologies start to help humans live easier and more tech-based lives, the part they play in the realm of healthcare is becoming significant. An already fast-paced, innovative and high investment industry is being propelled into the future by the coronavirus crisis, and as we have previously mentioned in our blog posts, the pandemic is accelerating digitalisation in medicine.

The roles and obligations according to the MDR

It is still the case that operators in the medical technology industry must implement the new regulations from EU Regulation 2017/745 (Medical Devices Regulation, MDR for short) by the deadline of 26 May 2021.

Medical device legislation

In terms of medical device legislation, we are in a transition period until 26 May, when the previously applicable Medical Device Directive (MDD) will be replaced by the new Medical Device Regulation (MDR) published in 2017.

Localization of medical and pharmaceutical texts

The European Union's new Medical Device Regulation (2017/745), or MDR, will become fully applicable in May 2021 and is expected to replace the existing Medical Device Directive (MDD) and Active Implantable Medical Devices (AIMD) Directives.

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